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本文引用的文献

1
Individuality in gut microbiota composition is a complex polygenic trait shaped by multiple environmental and host genetic factors.肠道微生物组成的个体差异是一种复杂的多基因特征,由多种环境和宿主遗传因素塑造。
Proc Natl Acad Sci U S A. 2010 Nov 2;107(44):18933-8. doi: 10.1073/pnas.1007028107. Epub 2010 Oct 11.
2
Incomplete recovery and individualized responses of the human distal gut microbiota to repeated antibiotic perturbation.人类远端肠道微生物组对重复抗生素扰动的不完全恢复和个体化反应。
Proc Natl Acad Sci U S A. 2011 Mar 15;108 Suppl 1(Suppl 1):4554-61. doi: 10.1073/pnas.1000087107. Epub 2010 Sep 16.
3
Impact of diet in shaping gut microbiota revealed by a comparative study in children from Europe and rural Africa.通过对欧洲和非洲农村儿童的比较研究揭示饮食对肠道微生物群的影响。
Proc Natl Acad Sci U S A. 2010 Aug 17;107(33):14691-6. doi: 10.1073/pnas.1005963107. Epub 2010 Aug 2.
4
Human milk glycobiome and its impact on the infant gastrointestinal microbiota.人乳糖组学及其对婴儿胃肠道微生物群的影响。
Proc Natl Acad Sci U S A. 2011 Mar 15;108 Suppl 1(Suppl 1):4653-8. doi: 10.1073/pnas.1000083107. Epub 2010 Aug 2.
5
Succession of microbial consortia in the developing infant gut microbiome.婴儿肠道微生物组中微生物群落的演替。
Proc Natl Acad Sci U S A. 2011 Mar 15;108 Suppl 1(Suppl 1):4578-85. doi: 10.1073/pnas.1000081107. Epub 2010 Jul 28.
6
Toll-like receptor 4 is protective against neonatal murine ischemia-reperfusion intestinal injury.Toll 样受体 4 可预防新生鼠肠缺血再灌注损伤。
J Pediatr Surg. 2010 Jun;45(6):1246-55. doi: 10.1016/j.jpedsurg.2010.02.093.
7
Composition, variability, and temporal stability of the intestinal microbiota of the elderly.老年人肠道微生物组的组成、变异性和时间稳定性。
Proc Natl Acad Sci U S A. 2011 Mar 15;108 Suppl 1(Suppl 1):4586-91. doi: 10.1073/pnas.1000097107. Epub 2010 Jun 22.
8
Delivery mode shapes the acquisition and structure of the initial microbiota across multiple body habitats in newborns.分娩方式影响新生儿多个身体栖息地初始微生物组的获得和结构。
Proc Natl Acad Sci U S A. 2010 Jun 29;107(26):11971-5. doi: 10.1073/pnas.1002601107. Epub 2010 Jun 21.
9
Vaginal microbiome of reproductive-age women.育龄期女性的阴道微生物组。
Proc Natl Acad Sci U S A. 2011 Mar 15;108 Suppl 1(Suppl 1):4680-7. doi: 10.1073/pnas.1002611107. Epub 2010 Jun 3.
10
Through ageing, and beyond: gut microbiota and inflammatory status in seniors and centenarians.随着衰老的发生以及之后:老年人和百岁老人的肠道微生物组和炎症状态。
PLoS One. 2010 May 17;5(5):e10667. doi: 10.1371/journal.pone.0010667.

人类胃肠道微生物组的发育和高通量测序的启示。

Development of the human gastrointestinal microbiota and insights from high-throughput sequencing.

机构信息

Department of Biology, University of Puerto Rico, Rio Piedras, San Juan, Puerto Rico.

出版信息

Gastroenterology. 2011 May;140(6):1713-9. doi: 10.1053/j.gastro.2011.02.011.

DOI:10.1053/j.gastro.2011.02.011
PMID:21530737
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10924805/
Abstract

Little was known about the development of the gastrointestinal (GI) tract microbiota, until recently, because of difficulties in obtaining sufficient sequence information from enough people or time points. Now, with decreased costs of DNA sequencing and improved bioinformatic tools, we can compare GI tract bacterial communities among individuals, of all ages from infancy to adulthood. Some key recent findings are that the initial bacterial community, even in the GI tract, depends strongly on delivery mode; that the process of early development of the microbiota is highly unstable and idiosyncratic; that the microbiota differs considerably among children from different countries; and that older adults have substantially different GI tract communities than younger adults, indicating that the GI tract microbiota can change throughout life. We relate these observations to different models of evolution including the evolution of senescence and suggest that probiotics be selected based on patient age. Studies of the microbiota in older people might tell us which probiotics could increase longevity. Drug metabolism varies among individuals with different microbial communities, so age- and region-specific clinical trials are required to ensure safety and efficacy.

摘要

直到最近,由于难以从足够多的人和时间点获取足够的序列信息,人们对胃肠道(GI)微生物组的发育知之甚少。现在,随着 DNA 测序成本的降低和生物信息学工具的改进,我们可以比较从婴儿到成年的各个年龄段个体的胃肠道细菌群落。一些最近的重要发现包括,即使在胃肠道中,初始细菌群落也强烈依赖于分娩方式;微生物组的早期发育过程极不稳定且具有个体差异;来自不同国家的儿童的微生物组差异很大;老年人的胃肠道群落与年轻人有很大不同,这表明胃肠道微生物组可以在整个生命周期中发生变化。我们将这些观察结果与包括衰老进化在内的不同进化模型联系起来,并建议根据患者年龄选择益生菌。对老年人的微生物组的研究可能会告诉我们哪些益生菌可以延长寿命。不同微生物群落的个体之间的药物代谢存在差异,因此需要进行年龄和地区特异性的临床试验,以确保安全性和有效性。